Novel connexin40 missense mutations in patients with familial atrial fibrillation. - Wikidata - wikimedia - TriplyDB

Novel connexin40 missense mutations in patients with familial atrial fibrillation.

Novel connexin40 missense mutations in patients with familial atrial fibrillation.

http://www.wikidata.org/entity/Q44343773

about

Emerging directions in the genetics of atrial fibrillation Targeted deep sequencing reveals no definitive evidence for somatic mosaicism in atrial fibrillation.A contemporary review on the genetic basis of atrial fibrillation.Degradation of a connexin40 mutant linked to atrial fibrillation is accelerated.Mutations in cardiovascular connexin genes.Low prevalence of connexin-40 gene variants in atrial tissues and blood from atrial fibrillation subjects Connexin40 abnormalities and atrial fibrillation in the human heart Atrial fibrillation-linked germline GJA5/connexin40 mutants showed an increased hemichannel function Molecular mechanisms regulating formation, trafficking and processing of annular gap junctions.Association of angiotensin-converting enzyme gene I/D and CYP11B2 gene -344T/C polymorphisms with lone atrial fibrillation and its recurrence after catheter ablation A variant in the carboxyl-terminus of connexin 40 alters GAP junctions and increases risk for tetralogy of Fallot.Genetic mechanisms of atrial fibrillation: impact on response to treatment The presence of two rare genomic syndromes, 1q21 deletion and Xq28 duplication, segregating independently in a family with intellectual disability.Atrial fibrillation: the role of common and rare genetic variants.Interfering amino terminal peptides and functional implications for heteromeric gap junction formation.Atrial fibrillation-linked GJA5/connexin40 mutants impaired gap junctions via different mechanisms.Genetic Discoveries in Atrial Fibrillation and Implications for Clinical Practice.Connexin Remodeling Contributes to Atrial Fibrillation.Atrial fibrillation-associated connexin40 mutants make hemichannels and synergistically form gap junction channels with novel properties.Genotype influence in responses to therapy for atrial fibrillation.An atrial-fibrillation-linked connexin40 mutant is retained in the endoplasmic reticulum and impairs the function of atrial gap-junction channels Human diseases associated with connexin mutations.Mutation spectrum of the GATA4 gene in patients with idiopathic atrial fibrillation.Phenotypic Variability Associated with a Large Recurrent 1q21.1 Microduplication in a Three-Generation Family Connexins in Cardiovascular and Neurovascular Health and Disease: Pharmacological Implications.Role of Non-Myocyte Gap Junctions and Connexin Hemichannels in Cardiovascular Health and Disease: Novel Therapeutic Targets?Functional Characterization of Novel Atrial Fibrillation-Linked GJA5 (Cx40) Mutants.Familial clustering of atrial fibrillation and comparative longitudinal outcomes of familial and non-familial atrial fibrillation

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Novel connexin40 missense mutations in patients with familial atrial fibrillation.

http://www.wikidata.org/entity/Q44343773

description

2010 nî lūn-bûn

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2010年の論文

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年学术文章

@zh-my

2010年学术文章

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2010年學術文章

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2010年學術文章

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2010年學術文章

@zh-hant

name

Novel connexin40 missense mutations in patients with familial atrial fibrillation.

@en

Novel connexin40 missense mutations in patients with familial atrial fibrillation.

@nl

type

label

Novel connexin40 missense mutations in patients with familial atrial fibrillation.

@en

Novel connexin40 missense mutations in patients with familial atrial fibrillation.

@nl

prefLabel

Novel connexin40 missense mutations in patients with familial atrial fibrillation.

@en

Novel connexin40 missense mutations in patients with familial atrial fibrillation.

@nl

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Novel connexin40 missense mutations in patients with familial atrial fibrillation.

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Hai-Feng Shi

http://www.w3.org/2001/XMLSchema#string

Hong-Wei Tan

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Wei-Feng Jiang

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Wei-Yi Fang

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Xian-Ling Zhang

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Xin-Hua Wang

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Xu Liu

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Yi-Qing Yang

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P2860

ACC/AHA/ESC 2006 Guidelines for the Management of Patients With Atrial Fibrillation

Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillation

Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation

Mutation in nuclear pore component NUP155 leads to atrial fibrillation and early sudden cardiac death

KCNQ1 gain-of-function mutation in familial atrial fibrillation

Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation.

Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation

Sodium channel mutations and susceptibility to heart failure and atrial fibrillation

Prevalence of diagnosed atrial fibrillation in adults: national implications for rhythm management and stroke prevention: the AnTicoagulation and Risk Factors in Atrial Fibrillation (ATRIA) Study

Atrial fibrillation as an independent risk factor for stroke: the Framingham Study

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1421-1427

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10.1093/EUROPACE/EUQ274

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atrial fibrillation